ENST00000266771.10:c.615A>G
MANE Select
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ENSP00000266771.5:p.Gly205=
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ENST00000266771.9:c.615A>G
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ENSP00000266771.5:p.Gly205=
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|
ENST00000366292.6:n.927A>G
|
|
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ENST00000376740.8:c.194A>G
|
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ENST00000376744.8:c.451A>G
|
|
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ENST00000535272.1:n.409A>G
|
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ENST00000539703.1:n.265A>G
|
|
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NM_145648.3:c.615A>G
|
NP_663623.1:p.Gly205=
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|
XM_011537895.1:c.765A>G
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XP_011536197.1:p.Gly255=
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XR_429081.2:n.638A>G
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XR_944494.1:n.788A>G
|
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XR_944495.1:n.788A>G
|
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XR_944496.1:n.788A>G
|
|
|
XR_944497.1:n.788A>G
|
|
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XM_017018791.1:c.765A>G
|
XP_016874280.1:p.Gly255=
|
|
XM_017018792.1:c.765A>G
|
XP_016874281.1:p.Gly255=
|
|
XM_017018793.1:c.615A>G
|
XP_016874282.1:p.Gly205=
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XR_002957287.1:n.638A>G
|
|
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XR_944496.2:n.788A>G
|
|
|
NM_145648.4:c.615A>G
MANE Select
|
NP_663623.1:p.Gly205=
|
|